EP0778893B1 - Bakterielle Produktion von Interferon-beta Polypeptiden - Google Patents

Bakterielle Produktion von Interferon-beta Polypeptiden Download PDF

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EP0778893B1
EP0778893B1 EP96919131A EP96919131A EP0778893B1 EP 0778893 B1 EP0778893 B1 EP 0778893B1 EP 96919131 A EP96919131 A EP 96919131A EP 96919131 A EP96919131 A EP 96919131A EP 0778893 B1 EP0778893 B1 EP 0778893B1
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ifn
polypeptide
cells
medium
concentration
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EP0778893A2 (de
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Glenn Dorin
Patrick J. Mcalary
Kathleen M. Wong
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Novartis Vaccines and Diagnostics Inc
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Novartis Vaccines and Diagnostics Inc
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00—Preparation of peptides or proteins
    • C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/52—Cytokines; Lymphokines; Interferons
    • C07K14/555—Interferons [IFN]
    • C07K14/565—IFN-beta

Definitions

  • This invention relates to the culturing of bacteria cells to produce a desired protein. Specifically, the invention relates to a method for the production of interferon- ⁇ ("IFN- ⁇ ") under certain culturing parameters, such as energy source, ion concentration, temperature, and pH.
  • IFN- ⁇ interferon- ⁇
  • IFN- ⁇ is the first identified effective treatment for those with MS. It is proven to reduce the number of attacks suffered by patients with relapsing and remitting multiple sclerosis ("MS"). Further, IFN- ⁇ is also being used to treat those patients with Hepatitis B or C.
  • IFN- ⁇ The amino acid and nucleotide sequence of IFN- ⁇ are known, as shown in Tanauguichi et al., Gene 10: 11-15 (1980 ).
  • Recombinant DNA technology makes it possible to produce IFN- ⁇ that is fee from viruses, e.g., HIV-1, and other contaminants from human sources.
  • IFN- ⁇ can be produced by culturing a host cell transformed with an expression vector that contains a gene encoding the amino acid sequence of IFN- ⁇ .
  • the host cell is one which can transcribe the gene and produce the desired protein.
  • IFN- ⁇ in mammalian, insect, and yeast host cells as described in, for example, Mantei et al., Nature (London) 297: 128 (1982 ); Ohno et al., Nucl. Acid Res. 10: 967 (1982 ); and Smith et al., Mol. Cell. Biol. 3: 2156 (1983 ).
  • muteins of IFN- ⁇ having improved characteristics have also been produced as described in, for example, Mark et al., US Patent No. 4,518,584 .
  • US Patent No. 4,499,188 is concerned with a process for bacterially producing a heterologous polypeptide such as IFN- ⁇ , comprising cultivating bacteria transformed to express said heterologus polypeptide under the control of a bacterial promoteroperator that
  • JP-A-62/282586 discloses the production of Cu-Zn-super oxide dismutase (SOD) by cultivating Escherichia coli harbouring the SOD gene in a culture medium containing casein hydrolyzate (e.g. peptone), yeast extract, inorganic salt (e.g. KCl), an assimilable carbon source (e.g. glucose) and, if necessary, CaCO 3 , CuSO 4 and ZnSO 4 .
  • casein hydrolyzate e.g. peptone
  • yeast extract e.g. KCl
  • an assimilable carbon source e.g. glucose
  • the invention relates to an improved method for producing IFN- ⁇ utilizing bacterial host cells capable of producing IFN- ⁇ . More specifically, the invention provides:
  • the method of the present invention relates to culturing conditions of Escherichia coli host cells capable of producing IFN- ⁇ polypeptide. These conditions lead to improved cell growth and product yields.
  • the host cell is transformed with an expression vector comprising the coding sequence of IFN- ⁇ polypeptide.
  • the expression vector can also contain if desired a promoter, terminator, origin of replication, and selectable marker. These components are known in the art and can be easily assembled.
  • Hydrophobic polypeptides comprise an abundance of hydrophobic amino acids, such as leucine, isoleucine, phenylalanine, and valine. Hydrophobic residues comprise approximately of 20% of the total residues in a hydrophobic polypeptide; more typically, approximately of 25% of the total residues; even more typically, approximately 30%. Hydrophobic polypeptides are capable of binding to other hydrophobic substances.
  • native IFN- ⁇ binds to hydrophobic substances such as Bule Dextran, Cibacron Blue F3GA-dextran, aminobenzene bound to agarose, aminonaphthalene bound to agarose, and aminoanthracene bound to agarose, ( Jankowski et al., Biochem.
  • hydrophobic proteins Another characteristic of hydrophobic proteins is the ratio of a helical to ⁇ -sheet residues. Hydrophobic proteins exhibit an ⁇ -helical to ⁇ -sheet ratio of approximately 2:1; more typically, a ratio of approximately 1.5:1; even more typically, approximately 1:1. The primary sequence of native IFN- ⁇ , a typical hydrophobic polypeptide, exhibits a ratio of approximately 1.1:1 according to Chou-Fasman analysis ( Hayes, Biochem. Biophys. Res. Commun. 95(2): 872-879 (1980 )).
  • IFN- ⁇ polypeptide can be utilized.
  • the term "interferon polypeptides" or “IFN- ⁇ polypeptides” refers to native IFN- ⁇ , muteins, analogs, and derivatives thereof. Such polypeptides which exhibit either the similar biological or receptor binding activity as the native IFN- ⁇ polypeptide. All of these IFN- ⁇ polypeptides will exhibit at least 60% of the receptor binding or biological activity of the native IFN- ⁇ . More typically, the polypeptides exhibit at least 75%, even more typically the polypeptides exhibit at least 80% of the native IFN- ⁇ receptor binding or biological activity. Biological and receptor binding assays are described in Fellous et al., Proc. Natl. Acad. Sci.
  • IFN- ⁇ polypeptides include mutants, fragments, fusions, analogs and derivatives of the native IFN- ⁇ . All of these polypeptides will exhibit some sequence identity to the native IFN- ⁇ .
  • Human IFN- ⁇ is one example of a native IFN- ⁇ . The human amino acid sequence of such is known and is further shown in SEQ ID NO:1. The polypeptides will retain at least about 80% amino acid identity with SEQ ID NO:1; more typically, at least about 85%; even more typically, at least about 90%.
  • the desired hydrophobic polypeptide can be constructed from known native sequences.
  • native IFN- ⁇ can be mutated to remove the cysteine that does not participate in disulfide bonding can be mutated to a serine using in vitro mutagenesis techniques.
  • Such mutagenesis is described in Mark et al., U.S. Patent No. 4,518,584 .
  • Other techniques for constructing fragments, fusion, analogs, and other derivatives are described in, for example, Sambrook et al., "Molecular Cloning: A Laboratory Manual” (New York, Cold Spring Harbor Laboratory, 1989 ).
  • the expression vector can be transformed into a Escherichia coli host cell. Transformation techniques are described in for example: Cohen et al. (1973) Proc. Natl. Acad. Sci. 69:2110 ; Dower et al. (1988) Nucleic Acids Res. 16:6127 ; Kushner (1978) "An improved method for transformation of Escherichia coli with ColEl-derived plasmids in Genetic Engineering: Proceedings of the International Symposium on Genetic Engineering (eds. H.W. Boyer and S. Nicosia ); Mandel et al. (1970) J. Mol. Biol. 53:159 ; and Taketo (1988) Biochim. Biophys. Acta 949:318 .
  • the preferred host cell and expression vector are deposited at the American Type Culture Collection in Rockville, Maryland, under ATCC no. 39517.
  • a host cell After a host cell is constructed, it is cultured under conditions effective to induce production of hydrophobic polypeptides. Such culture conditions include those that permit transcription and translation of the coding sequence to produce the desired hydrophobic polypeptide.
  • the cells may be in either lag, exponential growth, or stationary phase. Thus, the cells need not be rapidly dividing during the induction of polypeptide production.
  • Conditions that can affect bacterial production include, for example, aeration, pH, temperature, and medium composition.
  • media components which affect production include, for example, carbon sources, such as glycerol and glucose, trace elements, amino acids, cations, and anions.
  • the inventors herein have discovered certain conditions that dramatically increase the expression of IFN- ⁇ polypeptide in transformed Escherichia coli host cells. Such conditions include the concentration of potassium or sodium cations in the medium and the pH of the medium.
  • the potassium cation concentration is "low".
  • the potassium capon concentration of the present invention of the culture medium is no greater than 75 mM; more preferably, no greater than 40 mM.
  • the concentration of potassium is no less than 10 mM; more preferably, no less than 30 mM.
  • Potassium cations can be added to the culture medium discontinuously in batches or continuously to provide a continuous, low concentration of potassium ions or potassium salts. For convenience, the following concentrations are recommended to be added as a bolus at the beginning of the culturing.
  • the sodium cation concentration is "very low".
  • the sodium cation concentration herein is no greater than 100 ⁇ M; more usually, no greater than 50 ⁇ M.
  • no sodium cations are intentionally added to culture medium.
  • Sodium cations can be present in the medium, however, in the form of a contaminant from the vessel or from other components added.
  • the concentration of contaminating sodium is less than 100 ⁇ M.
  • non-sodium containing trace elements, phosphate salts, acids, and bases are used in the medium to limit the amount of sodium cations as much as possible.
  • ammonium hydroxide is preferable used herein in place of sodium hydroxide.
  • the Na + and K + cations from the other components of the medium such as, trace elements, phosphate salts, pH titrants, etc ., are taken in account. Because the concentrations of K + and Na + preferred are so low, a pH titrant such as NH 4 OH is preferred, to avoid adding K + and Na + cations.
  • an effective energy source must be provided to the cells during culturing and production of IFN- ⁇ polypeptide.
  • the energy source will not limit either the culturing time or final cell density or IFN- ⁇ polypeptide production.
  • the effective energy source can include a single or a mixture of compounds. As discussed below, glycerol and glucose are preferred energy sources. Other compounds, such fructose, maltose, etc., may also be effective.
  • Glycerol is the preferred effective energy source. Applicants have found when glycerol is utilized, the growth rate and the polypeptide production rate is increased. In one embodiment, the cells are fed only glycerol. Glycerol, however, need not be the only energy source present Energy sources that can be metabolized concurrently with glycerol may be present if they do not limit cell growth, culture time, or polypeptide production. For example, a small amount of glucose can be included in the culture medium with glycerol to reduce the lag phase of the cells. However, if production is linked to the tryptophan promoter, in a preferred embodiment of the present invention, then preferential metabolization of glycerol should begin just prior or at the time of tryptophan depletion. The amount of glucose, if any, should be limited under the circumstances.
  • glycerol when it is the carbon source, it is present in the medium at a concentration between 2g/L and 100g/L.
  • the concentration may be at least about 20 g/L, more typically, the glycerol concentration will be between about 20 g/L and about 100 g/L.
  • glycerol is available throughout the induction time.
  • the concentration of other energy sources, e . g ., glucose will be less than about 10 g/L; more usually, less than about 5 g/L; even more usually less than about 2.5 g/L.
  • the amount of glycerol added to the cells is not critical as long as the amount of glycerol does not limit the final cell density. Typically, a sufficient amount of glycerol will be at least 1 g/L. E. coli cells can tolerate glycerol concentrations up to 100 g/L.
  • the energy source can be supplied continuously or in batches throughout the culture period. Alternatively, the energy source can be supplied in one bolus at the beginning of the culture. For convenience, the cells are supplied with glycerol throughout the culture period.
  • glucose is fed at a limited rate. This feed strategy is unlike glycerol feed. Glucose is feed at or slightly less than the rate at which the cells metabolize the carbon source. One way to determine the limited rate of glucose is to monitor the polypeptide production for cultures with several glucose feed rates.
  • the inventors found that as the temperature during cell culture decreased, the protein production per cell increase.
  • the cells are typically grown at a temperature no less than 34°C; more usually, no less than 37°C; even more usually, no less than 39°C.
  • the cells are grown at a temperature no greater than 42°C; even more typically, no greater than 40°C.
  • the Escherichia coli host cells are therefore typically cultured at a temperature between 34°C and 42°C, for example 39.5°C.
  • Additional amino acids may not be necessary for culturing bacterial host cells. However, supplementing the culture with additional amino acids just prior and during induction of polypeptide production or during the terminal portion of the culture time may be useful. Supplementation of amino acids during culturing of bacterial cells to increase expression is described in U.S. Patent No. 4,656,132 and 4,894,334 . Also, feeding additional amino acids to the culture may be desired to limit incorporation of unwanted amino acids, such as nor-leucine. For example, nor-leucine incorporation can be restricted by feeding a limiting amount of leucine with an excess of isoleucine. Alternatively, threonine or valine can also be added to the culture medium to avoid nor-leucine incorporation. Other amino acids can also be supplemented to the medium so as not to limit the production of polypeptides.
  • Other fermentation conditions such as inoculation time and number of cells, will be chosen by convenience, and such factors are not critical to the claimed invention.
  • other medium components for inducing polypeptide production can include trace elements, carbon sources, vitamins, etc. Trace elements include copper, iron, manganese, zinc, magnesium, etc. Other carbon sources include amino acids, and lipids. These other media components are an example of the factors that are not critical to the invention and can be chosen for ease and convenience.
  • citrate and succinate are maintained in low concentrations during fermentation.
  • citrate and citrate salt concentrations are below 5 mM.
  • the cells can be harvested at any time after induction. Time-production studies can be performed to determine the time after induction when the cells have produced the most IFN- ⁇ .
  • IFN- ⁇ polypeptide producing cells can be harvested by (1) concentration of the cells, or (2) removal of unwanted media components before disrupting the cells. Specifically, the cells can be spun at 20,000 g at 4°C for 20 minutes, the supernatant removed, and then the cells can be resuspended at a concentration 100-200 OD 680 per mL in 0.1 M sodium phosphate, pH 7.4, 0.15 M NaCl in PBS. Alternatively, the cells can be concentrated five fold by circulating cross flow filtration, by circulating the material under pressure through a Millipore spiral ultrafiltration cartridge, for instance.
  • IFN- ⁇ polypeptide producing cells can be separated from the fermentation media by centrifugation and resuspension in a low ionic strength buffer.
  • the cells can be resuspended deionized water which optionally includes 1-2 mM EDTA, to chelate any remaining metal ions.
  • unwanted media components can be removed and the ionic strength lowered by diafiltering the cells against 5-10 volumes of deionized water which optionally includes 1-2 mM EDTA.
  • Other chelators can be used in place of EDTA, such as EGTA.
  • the first step of primary recovery is disrupting and optionally killing the cells producing IFN- ⁇ .
  • the isolated IFN- ⁇ polypeptide can be subjected to further processing, such as solubilization and denaturation procedures, or can be subjected to further purification of whole IFN- ⁇ refractile bodies, such as isolation by sucrose density centrifugation.
  • the cells producing IFN- ⁇ polypeptide can be disrupted by utilizing beads, high pressure homogenization or sonication.
  • disruption include homogenization at 6000-7000 psig, by either recycle mode or discrete pass mode (Preferably 3 passes at -10-15°C).
  • the cells can be disrupted by adding 0.2 ⁇ m beads as specified by Dynomill, mixing the beads and cells to disrupt the cells.
  • the cells can be disrupted by sonication using, e . g ., a Heat Systems Model W-375 at maximum power for five minutes.
  • the remaining undisrupted cells are killed.
  • the cells may be killed using phenol, toluene, or octanol, for example.
  • the addition of these reagents to the disrupted cells can cause physical changes to of the refractile bodies, such as density or hydrophobicity. These changes may be critical in the downstream processing purification of the desired IFN- ⁇ .
  • concentration of these reagents and the incubation time of these reagents with the disrupted cells can control the changes made to the refractile bodies.
  • disrupted cells that have produced IFN- ⁇ polypeptides can be incubated and agitated overnight with 1% (v/w) octanol at 0°C - 6°C to inactivate the residual cells.
  • the disrupted cells can be incubated with 0.25% (v/w) phenol and 0.25% (v/w) toluene for at least 30 minutes at about 37°C.
  • the ionic strength of the medium containing the disrupted cells can be lowered or the medium can be de-salted.
  • Such techniques and procedures for lowering the ionic strength of the medium before redisrupting the disrupted cells are described in U.S. Patent No. 4,748.234 .
  • the disrupted cells that have produced IFN- ⁇ polypeptide can be centrifuged at 20,000 g for 20 minutes at 4°C, and the pellet resuspended in deionized water which optionally includes 1-2 mM EDTA, to chelate the remaining ions.
  • deionized water which optionally includes 1-2 mM EDTA
  • EGTA can be added to between 1-2 mM to chelate the metal ions.
  • this mixture can be diafiltered against 5-10 volumes of deionized water with 1-2 mM EDTA.
  • Cellular debris can be dissociated from the refractile bodies by dispersing any aggregated material in the lysate by homogenization techniques. Homogenization techniques include sonication, mechanical agitation, or homogenization through a small aperture. For example, disrupted cells that produced IFN- ⁇ polypeptides can be dispersed again by sonication with a Heat Systems Model W-375 at maximum power for five minutes. Alternatively, the disruptate can be redispersed again passing it through a high pressure homogenizer three times at 6000-7000 psig.
  • the polypeptide refractile bodies can be further separated from the unwanted cellular components utilizing size or density differential methods. Low speed centrifugation is one method of separation. See Builder et al., U.S. Pat. No. 4,511,502 .
  • IFN- ⁇ polypeptide refractile bodies can be sedimented using sucrose density centrifugation to separate them from unwanted cellular material.
  • Factors which determine the effectiveness of the sucrose density centrifugation include the concentration of sucrose, the centrifugal force, and the residence time, or flow rate.
  • the final concentration of the sucrose is critical.
  • Using I-octanol may limit the percentage of IFN- ⁇ polypeptide refractile bodies which will sediment.
  • sucrose is added to a final density between 1.0 and 1.18 g/mL.
  • sucrose is added to the disruptate to a final density of 1.08 ⁇ 0.01 g/mL.
  • the refractile bodies either a continuous flow or lab centrifuge can be used. If a lab centrifuge is used, the IFN- ⁇ polypeptide refractile bodies, for example, are preferably spun at 8,000 g for at least 10 minutes. If a continuous flow centrifuge is used the centrifugal force, flow rate, and type of centrifuge are critical. For example, preferably, the mixture is centrifuged at 7,000 g at a flow rate of 0.25 L/minute in a Westfalia KA2 centrifuge or in a Sharples AS 16 centrifuge at 15,500 g at a flow rate of 2-3 L/min. The sedimented material, called particle paste, is collected.
  • a lab centrifuge the IFN- ⁇ polypeptide refractile bodies, for example, are preferably spun at 8,000 g for at least 10 minutes.
  • a continuous flow centrifuge the centrifugal force, flow rate, and type of centrifuge are critical. For example, preferably, the mixture is centrifuged at
  • centrifuges If these centrifuges are used, they must be stopped to collect the refractile bodies from the centrifuge bowl. With a continuous flow centrifuge, the supernatant is continuously discharged. Other types of lab or continuous centrifuges may be utilized, and it is recognized that those skilled in the art can make the needed adjustments to centrifugal force and flow rate, for example, with these different centrifuges to produce an effective homogeneous sucrose cushion.
  • IFN- ⁇ can be isolated effectively utilizing organic phase extraction.
  • IFN- ⁇ polypeptides can be effectively isolated from contaminants by organic extraction with a aliphatic alcohol.
  • Such extraction methods are described in Konrad et al., U.S. Pat. No. 4,450,103 ; and Hanisch et al., U.S. Pat. No. 4,462,940 .
  • this type of extraction is effective at removing unwanted endotoxins.
  • the extraction for IFN- ⁇ polypeptides is more effective if the IFN- ⁇ polypeptides are solubilized with a strong anionic detergent before extraction and if the detergent is present during extraction.
  • the strong anionic surfactant apparently increases partition efficiency during organic extraction reducing the cross-linking of contaminating proteins to the desired hydrophobic polypeptides.
  • Strong natural or synthetic anionic surfactants such as alkali metal salts of fatty acids and alkali metal alkyl sulfates, are preferred for solubilization before organic extraction.
  • Such agent will usually contain 10 to 14 carbon atoms.
  • Sodium dodecyl sulfate (SDS) and sodium laurate are particularly preferred solubilizing agents.
  • solubilizing agents examples include but are not limited to sodium dodecyl sulfonate, sodium dodecyl sulfate, sodium tetradecyl sulfate, sodium tridecyl sulfonate, sodium myristate, sodium caproylate, sodium dodecyl N-sarcosinate, and sodium tetradecyl N-sarcosinate.
  • solubilizing agent used in the solubilization depends upon the particular agent and the amount of protein to be solubilized. Typically, sufficient solubilizing agent to protein weight ratios range from about 1:1 to 10:1. When SDS is used, a SDS to protein ratio of about 1:1 to 10:1, preferably about 7:1 to 2.5:1, is used. Temperatures in the range of 15°C to 60°C, are normally used in the solubilization.
  • the solubilization is considered complete when the solution is substantially clear. For example, when the OD 280 of the solution reaches about 4.0 to 8.0, the solubilization process is considered complete.
  • a reducing agent for complete solubilization of the refractile bodies, the addition of a reducing agent is recommended.
  • Dithiothreitol, fi-mercaptoethanol, and thioglycolic acid are examples of reducing agents.
  • the above reducing agents preferably are utilized at about 50 mM. Extremes in pH and/or temperature can facilitate or cause solubilization. IFN- ⁇ polypeptides as an example, adjusting the pH to between 9.0 to 11.0 in the solubilization buffer. Heating the mixture to 50°C to 55°C or as high as 95°C for at least twenty minutes will facilitate solubilization. The time of solubilization will be lengthy if the refractile bodies are too concentrated.
  • the protein concentration can range between 3-8 mg/mL, and the solubilization will proceed efficiently.
  • solubilization and reduction of refractile bodies is efficient at protein concentrations of 0.5 to 25 mg/mL.
  • a chelating agent such as EDTA, EGTA, or citrate
  • EDTA EDTA
  • EGTA EGTA
  • citrate a chelating agent
  • IFN- ⁇ polypeptides typical hydrophobic polypeptides, the following concentrations are recommended, 2mM EDTA, 2mM EGTA, or 5 mM citrate.
  • the ionic strength of the solution is adjusted, if necessary, to a level at which the solution and organic extractant will be substantially immiscible.
  • the ionic strength will be in the range of 0.05 to 0.15.
  • Inorganic salts, such as NaCl, may be added to the solution for this purpose.
  • Such ionic strengths enable phase separation after the extraction.
  • the extractants used in the process are 2-butanol, 2-methyl-butanol, or mixtures, thereof.
  • the mixtures preferably contain less than about 50% by volume 2-methyl-butanol.
  • 2-butanol is a preferred extractant for IFN- ⁇ polypeptides. Homologous alcohols were found to be ineffective extractants.
  • the extractant will normally combined with the aqueous solution of IFN- ⁇ polypeptide in volumetric ratios in the range of about 0.8:1 to about 3:1, preferably about 1:1 (extractant:aqueous solution).
  • the extraction may be carried out using conventional batch or continuous liquid-liquid extraction techniques and equipment.
  • the extraction will normally be carried out at 20°C to about 100°C.
  • the extraction will involve contact times in the range of about one minute to one hour. The optimum contact time will depend upon the particular solubilizing agent:extractant combination. When SDS is used, shorter times in the above range may be used. When sodium laurate is used, longer times in the range are expected.
  • the pH of the extraction mixture will range between about 6 and 9, with a pH of about 7.5 being preferred when SDS is used, and a pH of about 8.5 when sodium laurate is used.
  • the aqueous phase and extractant phase are separated, and the IFN- ⁇ is isolated from the extractant phase.
  • the particular isolation procedure to be used will depend upon the solubilizing agent involved and the desired degree of purity.
  • Various isolation techniques such as precipitation, molecular sieve chromatography, affinity chromatography, and electrophoresis may be employed.
  • SDS utilized with IFN- ⁇ polypeptide other proteins can be precipitated from the extractant mixed with aqueous buffer at volumetric rations of about 2:1 to about 5:1, preferably about 3:1, by reducing the pH, typically to between 5 to 7, more typically about 6.5.
  • the organic extract containing IFN- ⁇ polypeptide can be mixed with a buffer containing 0.1% SDS, in 10 mM phosphate, 0.9% saline, pH 7.4 and DTT is added to a final concentration of 5 mM to ensure that the IFN- ⁇ polypeptide remains in a reduced monomeric state. The mixture is allowed to come to about 20°C.
  • the pH organic extract can be adjusted to about 6.2 ⁇ 0.1 to precipitate the IFN- ⁇ polypeptides.
  • the precipitate can be collected by centrifugation or filtration. For example, the precipitate isolated by centrifuging the mixture at with a Sharples AS 16 centrifuge at 15,500 g at a flow rate of 2-3 L/min.
  • the precipitate can be resuspended in a buffer solution that is convenient for further purification procedures or refolding reactions.
  • Refolding and oxidiation conditions will vary from polypeptide to polypeptide. Typically, the polypeptide will be solubilized and reduced to monomer form before oxidation and refolding. The following are specific conditions for refolding IFN- ⁇ polypeptides.
  • IFN- ⁇ polypeptide resulting from the solubilizing of IFN- ⁇ refractile bodies can be refolded and oxidized into biologically active conformation under a range of conditions as shown in Mark et al., U.S. Patent No. 4,518,584 .
  • IFN- ⁇ polypeptide may be refolded at a concentration as high as I mg/mL. This concentration may be preferred when the reaction vessel volume and buffer material are limited. However, the IFN- ⁇ polypeptide can be refolded at a concentration as low as 0.01 mg/mL. The concentration of IFN- ⁇ for refolding is also dependent on the amount of contaminant present.
  • the concentration of contaminating material the lower the concentration of IFN- ⁇ polypeptide is required for efficient refolding.
  • concentration of IFN- ⁇ polypeptide is 0.13 mg/mL.
  • IFN- ⁇ polypeptide can be easily refolded without an additional oxidation reagent by removing the reducing agent(s), if one is present, and allowing oxidation with atmospheric oxygen. As shown in Example 8 of Mark et al., U.S. Pat. No. 4,518,584 .
  • the oxidation buffer may contain a chelator, such as 1 mM EDTA or 1 mM EGTA, to prevent unwanted oxidation by metal ion contaminants. Obviously, chelators are not desired when copper ions are the oxidation reagent.
  • a chaotropic agent can also be included in the oxidation buffer to reduce the amount of IFN- ⁇ polypeptide oligomers that are produced by the oxidation reaction.
  • the chaotropic agent should not be such a high concentration that it prevents refolding altogether.
  • Useful chaotropic agents include 0.1 % SDS, 2 M urea, and 2 M guanidine hydrochloride.
  • IFN- ⁇ polypeptide was added in equimolar amounts to iodosobenzoic acid (IBA) into a reaction vessel containing 2 mM sodium pyrophosphate, 0.1 % SDS and 1 mM EDTA.
  • the pH was controlled during oxidation at 9.0 ⁇ 0.1 with 0.5 N NaOH and adjusted to 5.5 ⁇ 0.2 when oxidation was complete.
  • IFN- ⁇ polypeptide can be added in equimolar amounts to 15 ⁇ m IBA, 2 mM pyrophosphate, 0.1% SDS, and 1 mM EDTA buffer over 5 hours. The pH is maintained at 9.0 ⁇ 0.1 with NaOH. Next, iodosobenzoic acid is added to a 20 ⁇ M excess for an additional hour. The reaction can be terminated after about 7 to 7.5 hours by lowering the pH to between 5.2 and 5.7. The IFN- ⁇ polypeptide can undergo multiple oxidation reactions to increase the amount of refolded IFN- ⁇ polypeptide.
  • IFN- ⁇ polypeptides can be isolated based on charge, size or hydrophobicity characteristics. Specific examples of useful columns are high pressure liquid chromatography (HPLC), reverse phase HPLC, and Sephacryl®. Several column runs or column types may be needed to remove the contaminants. The number or type of columns will be chosen according to the desired purification, timing, and financial parameters. The specific procedure chosen is not critical to the practice of the invention. Further, column chromatography may take place before or after refolding of the IFN- ⁇ polypeptide. Column chromatography is beneficial before refolding to remove contaminants which may interfere or limit IFN- ⁇ polypeptide refolding efficiency.
  • HPLC high pressure liquid chromatography
  • reverse phase HPLC reverse phase HPLC
  • Sephacryl® Sephacryl®
  • One column chromatography procedure utilizes two Sephacryl® columns.
  • the IFN- ⁇ polypeptides are subjected to a Sephacryl® S-200 and then to a Sephacryl® G-75 column for a final purification to attain 99% purity.
  • IFN- ⁇ polypeptide refractile bodies was extracted with an organic solvent and acid precipitated.
  • the IFN- ⁇ polypeptides are chromatographed on dual 2.6 x 80 cm columns packed with Sephacryl S-200 Superfine. Columns are equilibrated and eluted with 50 mM sodium acetate, pH 5.5 2 mM DTT, and 0.5 mM EDTA. Sample volumes of 10-20 mM (5-10 mg protein/mL) and flow rates of 1-2 ml/minutes are recommended. Protein elution can be monitored by absorbance at 280 nm and biological activity can be quantitated by interferon assay (CPE).
  • CPE interferon assay
  • Another IFN- ⁇ polypeptide column chromatography procedure utilizes three Sephacryl® columns, using a Sephacryl® S-200 column run before and after refolding and a final Sephacryl® G-75 to attain the desired level of purity.
  • the solubilized IFN- ⁇ polypeptide refractile bodies Prior to chromatographic isolation, the solubilized IFN- ⁇ polypeptide refractile bodies are extracted by organic solvent and acid precipitated.
  • the IFN- ⁇ polypeptide precipitate is resolubilized and treated with a reducing agent, such 20 mM DTT or 10 mM ⁇ -mercaptoethanol, to maintain the IFN- ⁇ polypeptide in the reduced, monomeric state.
  • a reducing agent such 20 mM DTT or 10 mM ⁇ -mercaptoethanol
  • the IFN- ⁇ polypeptide precipitate can be resuspended with a chaotropic agent, such as 5% SDS or 6M urea, to monomeric IFN- ⁇ polypeptides.
  • chelators such as 5 mM EDTA or 5 mM EGTA, can be added to scavenge metal ions which can promote oxidation of sulfhydryl groups.
  • Useful buffers include 50 mM sodium phosphate or 50 mM Tris-HCl.
  • the pH is adjusted to 8.5 ⁇ 0.1 with sodium hydroxide and the solution is heated to between 45°C to 55°C for about 10 minutes, to facilitate reduction.
  • the mixture is cooled to below 30°C and the pH is adjusted to between 5.2 to 5.8 with glacial acetic acid and filtered through a 0.2 ⁇ m Sartobran capsule filter.
  • Sephacryl S-200 Superfine is a gel filtration liquid chromatography medium which is prepared from covalently linked allyl dextran and N,N'-methylenebisacrylamide with an exclusion limit of 250,000.
  • the S-200 is packed into six section Pharmacia stacked columns. The column is first equilibrated with NLT 80 L of 50 mM acetate buffer, 1% SDS, 1 mM EDTA, pH 5.5. The column is loaded with solubilized IFN- ⁇ polypeptide extracted with organic solvent and acid precipitated. The IFN- ⁇ polypeptide is eluted from the column with 50 mM acetate, 1% SDS, 1 mM EDTA, pH 5.5.
  • the IFN- ⁇ polypeptide is refolded, it is loaded and eluted from a Sephacryl® S-200 column according to the conditions described above.
  • the desired fractions are pooled and concentrated to less than 4 L using an Amicon ultrafiltration cartridge.
  • Sephadex® G-75 is a bead-formed, crosslinked dextran gel filtration medium.
  • the column is equilibrated with NLT 80 L of 50 mM acetate buffer, 0.1% SDS, 1 mM EDTA, pH 5.5.
  • the column is loaded with not more than 8 g of protein and the IFN- ⁇ polypeptide is eluted with the equilibration buffer.
  • the pooled fractions containing IFN- ⁇ polypeptide may be held at 2-8 °C for up to 6 months or at -20°C or colder for one year prior to formulation.
  • the formulation can be chosen based on convenience. The following can be used to formulate IFN- ⁇ polypeptides for lyophilization.
  • the purified IFN- ⁇ polypeptide is formulated by adding the appropriate sterile components to protect the IFN- ⁇ polypeptide during all stages of storage and use.
  • the IFN- ⁇ polypeptides obtained in accordance with this invention may be formulated either as a single product or mixtures of the various IFN- ⁇ polypeptides.
  • the IFN- ⁇ polypeptides are formulated with pharmaceutically acceptable preparations a physiologically compatible carrier media for clinical and therapeutic uses.
  • Other physiologically compatible compounds may also be included in the formulation, such as dextrose, human serum albumin, etc .
  • the IFN- ⁇ formulation can contain a concentration IFN- ⁇ polypeptide between 0.25 mg/mL to 15 mg/ml.
  • the amount of IFN- ⁇ polypeptide included in the formulation is not critical to the invention and will depend on the dosage to given for a particular indication and delivery regimen.
  • Sugars can be utilized in formulating IFN- ⁇ polypeptides include mannitol, dextrose, and sucrose.
  • concentration of mannitol is between 1% (wt/v) and 5% (wt/v); more typically, the concentration is approximately 2.5%.
  • concentration is between 0.5% (wt/v) and 2% (wt/v); more usually, the concentration is approximately 1.25% (wt/v).
  • sucrose concentration is between 1% (wt/v) and 5% (wt/v); more usually, the concentration is approximately 1.75%.
  • amorphous protectants examples include dextran, trehalose, 2-hydroxypropyl-p-cyclodextrin, amino acids, such as glycine, or human serum albumin. These protectants help reduce the physical and chemical alterations to the IFN- ⁇ polypeptides, such as oxidation, etc .
  • An effective amount of amorphous protectant will prevent unwanted aggregation, chemical linkage, oxidation and degradation of IFN- ⁇ polypeptide. Too much amorphous protectant will hinder efficient lyophilization, and too little will reduce the shelf life of lyophilized product.
  • Glycine can be added to the IFN- ⁇ polypeptide formulation to a final concentration of at least 0.01% (wt/v), more usually at least 0.3% (wt/v).
  • the glycine concentration in the formulation is no more than 1% (wt/v), more preferably no more than 0.7% (wt/v).
  • HSA Human serum albumin
  • IFN- ⁇ polypeptide formulation can also be added to the formulation as a protectant.
  • HSA is added to the IFN- ⁇ polypeptide formulation to a final concentration of at least 0.01% (wt/v), more usually at least 0.5% (wt/v).
  • the glycine concentration in the formulation is no more than 2.5% (wt/v), more preferably no more than 1.25% (wt/v).
  • Buffers can be utilized to maintain the pH of the formulation during lyophilization, storage, and once the IFN- ⁇ polypeptide is reconstituted. Maintenance of pH is critical to prevent such physical and chemical alterations, such as oxidation, during storage of the IFN- ⁇ polypeptide.
  • the pH will be chosen not only to optimize the longevity of the IFN- ⁇ polypeptide but to ease administration of the IFN- ⁇ polypeptide to humans.
  • the pH of the formulation is adjusted to between 6.0 and 7.5 with NaOH if a sodium containing buffering reagent is used. More preferably the pH is adjusted to 6.5.
  • Sodium citrate or phosphate are examples of amorphous buffers.
  • Sodium citrate is added to the formulation to a final concentration of at least 1 mM, and more preferably at least 4 mM.
  • concentration of sodium citrate in the formulation is no more than 10 mM, and more typically no more than 6 mM.
  • IFN- ⁇ polypeptides are formulated as desired, such a formulation can be stored as a frozen liquid or lyophilized.
  • the form for storage of an IFN- ⁇ polypeptide formulation is not critical for the instant invention and chosen for convenience.
  • U.S. Patent 5,183,746 describes IFN- ⁇ liquid formulations that are stored as frozen liquids instead in the lyophilized form.
  • frozen liquid formulations can contain glycerol and a combination of biocompatible non-ionic polymeric detergents and a small amount of buffer to maintain the formulation at the desired pH.
  • Preferred concentrations of glycerol are from about 0.005% to about 5%; more preferably, from about 0.01% to about 3%; even more preferably from about 0.05% to about 1.5%.
  • glycerol is present in the liquid formulations at a concentration range by volume of from about 5% to about 50%, preferably from about 20% to about 30% and more preferably about 25%
  • the combination of non-ionic detergents acting with the glycerol can be added to a lower concentration
  • the preferred concentration are from about 0.0005% to about 5%, preferably, from about 0.001% to about 1%, and more preferably, from about 0.01% to about 0.5%.
  • a preferred detergent is SDS.
  • the liquid formulation may lyophilized according to techniques known in the art.
  • lyophilization procedure comprise a freezing step, a primary drying step, and a secondary drying step.
  • the formulation is frozen in order to:
  • freezing temperature is below 0°C; more typically, below -20°C; even more typically, the formulation is frozen below -50°C.
  • the vials containing the formulation can be frozen in the lyophilizer at atmospheric pressure.
  • the temperature of the formulation is controlled by the shelf temperature in the lyophilizer.
  • the vials are placed on a pre-cooled shelf, 10°C, for example, and then the shelf temperature is lowered to freeze the formulation.
  • the temperature can be lowered at a rate of between 33°C per hour and approximately, 45°C per hour.
  • the formulation should be held at the desired temperature for about 30 minutes to two hours or more.
  • the formulation is dried in two steps, primary and secondary drying.
  • the chamber pressure is reduced below atmospheric pressures to force the water to proceed directly from solid to gas phase, i . e., sublimate.
  • the primary drying begins after the formulation is frozen, and most of the water is removed by this step.
  • the pressure in the sample chamber is reduced, and the shelf temperature of the lyophilizer is raised and held constant at a primary drying temperature.
  • the shelf temperature is held constant to allow the product temperature to equilibrate with the shelf temperature as shown in Figure 1 on page 49 of Williams et al ., supra .
  • the water vapor is discharged into the condenser of the lyophilizer, which re-freezes the vapor.
  • Subatmospheric pressures refer to any pressure below one atmosphere unit.
  • the subatmospheric pressure will between 500 and 10 ⁇ mHg; more preferably between 200 to 50 ⁇ m Hg; even more preferably about 70 ⁇ mHg.
  • the liquid formulation or frozen product temperature is adjusted by changing the shelf temperature of the lyophilizer.
  • the sample temperature whether the sample is solid or liquid, usually lags behind the shelf temperature.
  • the sample temperature can be changed to a target temperature by two techniques. First, the shelf temperature may be changed and held constant at a target temperature until the sample equilibrates with the shelf temperature. Or the shelf temperature can be adjusted slowly to a target temperature so that the temperature difference between the shelf and the sample is minimal. Either method is effective for changing the sample temperature. The choice of techniques will depend on the desired rate of temperature change. However, the temperature should not be increased so quickly that the water evaporates instead of lyophilizes from the product.
  • the shelf temperature is raised to between about -20°C and -5°C for primary drying.
  • the temperature is raised to the primary drying temperature at a rate of between about 30°C per hour to about 60°C per hour.
  • the formulation is held at the desired primary drying temperature between about 3 to 15 hours.
  • the shelf temperature is raised to a secondary drying temperature and then held constant.
  • the shelf temperature is held constant to allow the product temperature to equilibrate with the shelf temperature.
  • water which is tightly bound to the product is removed.
  • the shelf temperature is raised to between about 15°C and 30°C for secondary drying.
  • the temperature is raised to the secondary drying temperature at a rate of between about 30°C per hour to about 60°C per hour.
  • the formulation is held at the desired primary drying temperature somewhere between about 3 to 15 hours.
  • the vials can be stoppered under pressure with a variety of gases.
  • the chamber can be pressurized between 12 psi with the desired gas. Gases that limit the chemical modification of IFN- ⁇ polypeptides are preferred, such as N 2 .
  • An Escherichia coli host cell was transformed with an expression vector containing a gene encoding an IFN- ⁇ polypeptide.
  • the encoded IFN- ⁇ polypeptide has the same sequence as SEQ ID NO:1 except it has a serine in place of a cysteine at position 17 of SEQ ID NO: 1.
  • the construction of this cell line is described in Mark et al., U.S. Patent No. 4,518,584 .
  • the human IFN- ⁇ gene was isolated, modified and transferred into a prokaryotic host, E. coli , creating a cell capable of IFN- ⁇ polypeptide production.
  • the native IFN- ⁇ gene was modified to encode a protein which has a serine in place a cysteine at amino acid position 17, according to SEQ ID NO:1.
  • This modification was made to preclude the formation of IFN- ⁇ polypeptides with undesirable tertiary structure due to incorrect disulfide bonding between cysteine residues.
  • the cysteine 17 does not participate in disulfide bonding in the active native human IFN- ⁇ polypeptide.
  • site-directed mutagenesis was used to substitute a serine in place of the cysteine to prevent unwanted disulfide bonding.
  • the native human IFN- ⁇ gene was isolated and its leader peptide sequences deleted.
  • the E. coli trp promoter sequence was isolated and vector incorporating these components was constructed.
  • the IFN- ⁇ gene was subcloned into bacteriophage M13mp8 to produce a single stranded DNA containing the native human IFN- ⁇ coding sequence.
  • the codon for the amino acid cysteine at position 17 was modified to encode a serine.
  • the phage DNA containing the serine modified IFN- ⁇ polypeptide gene was isolated.
  • the modified gene was excised from the phage DNA and inserted into a vector containing a correctly oriented E. coli trp promoter.
  • This vector was designated plasmid pSY2501.
  • E . coli strain MM294-1 were transformed with this plasmid to create a cell capable of producing an IFN- ⁇ polypeptide.
  • a clone, 4E1 was used containing the complete sequence encoding the native mature human IFN- ⁇ protein and its leader peptide.
  • the gene was isolated by digesting the clone with HhaI restriction enzyme and the 1.2 kilobase double stranded HhaI fragment containing the IFN- ⁇ sequence was melted to separate the DNA into single stranded cDNA.
  • a synthetic oligonucleotide with the sequence TATGAGCTACAAC (SEQ ID NO:2) was used to hybridize to the DNA adjacent to the leader peptide sequence.
  • the 5' end of the oligonucleotide began with the base T in order to regenerate a Hind III sight preceding the initiation codon ATG.
  • DNA polymerase I treatment (3' to 5' exonucleolytic activity) removed the single stranded DNA coding for the leader peptide.
  • the enzyme's polymerase activity then restored the native human IFN- ⁇ sequence to a double stranded cDNA with a 5' blunt ended terminus.
  • PstI restriction enzyme was used to cleave the repaired DNA, resulting in a 144 base pair (bp) fragment encoding the N-terminus portion of the native human IFN- ⁇ gene.
  • the IFN- ⁇ cDNA was now a 5' blunt ended fragment beginning with the base T, followed by the initiation codon ATG which codes for the mature protein's N-terminus methionine, and ending at the PstI site of the gene.
  • the fragment encoding the C-terminus of the native human IFN- ⁇ sequence was isolated from the original clone 4E1 by digesting it with Pst I and Bgl II restriction enzymes and recovering the 359 bp Pst I -Bgl II fragment.
  • plasmid pBR322 was cleaved with Hind III restriction enzyme, followed by DNA polymerase I treatment to blunt-end the Hind III site. Bam HI restriction enzyme was then used to remove a portion of the open plasmid as a repaired Hind III -Bam HI fragment.
  • the N-terminus and C-terminus encoding IFN- ⁇ fragments were then inserted into the prepared pBR322 in a three way ligation: the repaired 5' end of the IFN- ⁇ N-terminus fragment was blunt-ended ligated to the repaired Hind III site, the 3' Pst I end of the N-terminus fragment and the 5' Pst I end of the C-terminus encoding fragment were ligated, and the 3' Bgl II site of the C-terminus encoding fragment was ligated to the Bam HI cohesive end in pBR322 to create an Xho II site. The resulting clone was designated p ⁇ 1-25.
  • Plasmid ptrp3 was the source for the trp promoter.
  • the trp promoter was isolated from ptrp3 by cleaved with Eco RI and Hind III restriction enzymes. These enzymes were also used to cleave plasmid p ⁇ 1-25, removing the intervening Eco RI -Hind III sequence. The fragment containing the trp promoter was ligated into p ⁇ 1-25 as an Eco RI -Hind III fragment. The resulting clone, designated p ⁇ 1-trp.
  • restriction enzymes Hind III and Xho II were used to excise the native human IFN- ⁇ coding sequence from plasmid p ⁇ 1-trp.
  • a short section of double stranded, Replicative Form (RF) M13mp8 phage DNA was removed by cleavage with restriction enzymes Hind III and Bam HI to accommodate with the IFN- ⁇ sequence which was then ligated into place.
  • Sites cleaved with Xho II and Bam HI have compatible sticky ends; in this case the resultant ligation regenerated the Xho II site.
  • the recombinant phage DNA was transformed into competent cells of E.
  • M13- ⁇ 1 coli strain JM103, which is a strain commonly used for the production of M13 phage DNA. Restriction enzymes were used to identify RF clones containing the IFN- ⁇ gene. One such clone, designated M13- ⁇ 1 was used to prepare single stranded phage DNA to serve as the template for site specific mutagenesis.
  • the required mutation was accomplished by manufacturing a synthetic oligonucleotide primer whose sequence: GCAATTTTCAGAGTCAG (SEQ ID NO:3) is identical to a seventeen nucleotide sequence in the sense strand of IFN- ⁇ around the region of codon 17, except for a single base pair mismatch.
  • This mismatch at nucleotide 12 of the primer substituted A for the native T, resulting in the substitution of serine for cysteine at amino acid position 17.
  • the base substitution also created a new HinFI site, which facilitated detection of the serine-17 mutation.
  • Hybridization of the synthetic primer to the phage DNA was followed by primer extension, using DNA polymerase I Klenow fragment to form double stranded DNA (RF) which was used to transform competent cells of E. coli strain JM103. Transformed E. coli colonies extruded single stranded progeny phage whose DNA encoded either the mutated IFN- ⁇ ser17 sequence, or the native human IFN- ⁇ polypeptide. Selection for phage progeny carrying the mutated IFN- ⁇ gene was carried out using a 32P-labeled form of the above synthetic primer as a probe. The probe was fully complementary to the DNA region containing the Cys 17 to Ser 17 mutation, and therefore hybridized most strongly to phage DNA carrying the mutation.
  • M13-SY2501 One phage clone that hybridized to the probe was designated M13-SY2501; detection of the new HinfI restriction site in this clone also indicated the presence of the correct single base mutation. Dideoxy sequencing of the single stranded form of M13-SY2501 confirmed that the TGT Cys codon was converted to an AGT Ser codon.
  • the mutated IFN- ⁇ gene was excised from phage M13-SY2501 RF DNA by cleaved with Hind III and Xho II. Plasmid ptrp3 containing the E. coli trp promoter was cleaved with Hind III. and Bam HI, which removed a portion of DNA just 3' to the trp promoter. This inactivated the plasmid gene for tetracycline resistance. The IFN- ⁇ ser17 fragment was then ligated into the Hind III and Bam HI sites of ptrp3 with T4 DNA ligase, and the ligated DNA was transformed into E. coli strain MM294.
  • Plasmid pSy2501 was transformed into a competent subvariant E. coli strain MM294 designated MM294-1 and expression of IFN- ⁇ ser17 was verified. Samples of the transformed cells were deposited in the Cetus Master Culture Collection and the American Type Culture collection, Rockville, Maryland, under ATCC no. 39517.
  • the IFN- ⁇ ser17 gene is under the control of a trp promoter and is present within E. coli as a multicopy plasmid. Expression of the gen is determined by the intracellular level of tryptophan. Molecules of this amino acid form complexes with the intracellular trp repressor protein and this complex binds to the operator region of the trp promoter/operator, preventing IFN- ⁇ ser17 gene transcription. Therefore, in the presence of an intracellular source of tryptophan, IFN- ⁇ ser17 production is repressed. During culture growth, the extracellular tryptophan is consumed and its concentration drops.
  • the rate of tryptophan consumption is proportional to the amount of cell growth, the cell density at which the tryptophan is fully consumed may be predicted.
  • the promoter/operation region is freed from the trp repressor/tryptophan complex and the RNA polymerase is able to transcribe the IFN- ⁇ ser17 gene.
  • the cloned trp promoter includes a ribosome binding site sequence so that the transcribed IFN- ⁇ ser17 mRNA is translated by E. coli ribosomes. Because the same trp promoter system also controls the expression of the proteins needed to biosynthesize tryptophan, the cells can maintain an adequate supply of tryptophan even without an extracellular source.
  • Plasmid ptrp3 was created by subcloning the E. coli trp promoter from plasmid pVV1 as a repaired (blunt-ended) Hha I -Taq I partial fragment of 100 bp. It was inserted into the repaired (blunt-ended) Eco RI -Cla I sites of pBR322, regenerating both the Eco RI and Cla I sites.
  • the strain used for production of IFN- ⁇ ser17 is an E. coli K-12 strain known as MM294-1, which was originally derived from strain MM294.
  • the strain has no special nutritional requirement except thiamine, allowing it to grow rapidly on thiamine-supplemented minimal medium in fermentors.
  • the variant MM-294 was isolated from a IFN- ⁇ producing clone of MM294 which had been transformed with the IFN- ⁇ plasmid pSY201, and differs from MM294 in the level of expression of the IFN- ⁇ gene.
  • the pSY2101 plasmid expressed IFN- ⁇ at higher levels in this culture than in other MM294 clones. It was necessary to remove the pSY2101 plasmid, which encoded the native human IFN- ⁇ polypeptide with Cys 17 .
  • the bacterium was cured of the pSY2101 plasmid by culturing under expressing conditions and replica plating, selecting for colonies which had lost antibiotic resistance.
  • the isolate host was renamed MM294-1.
  • the recovered product was assayed for native, human IFN- ⁇ activity using an assay based on viral protection.
  • the procedure was performed in microtiter plates. First, 50 ⁇ L of minimum essential medium were charged into each well, and 25 ⁇ l of the sample was placed in the first well, and 1:3 volume dilutions were made serially into the following wells. Vesicular Stomatitis virus, human fibroblast cell line GM-2767, and reference IFN- ⁇ controls were included on each plate. The reference IFN- ⁇ used was 100 units per mL. The plates were then irradiated with UV light for 10 minutes.
  • IFN- ⁇ polypeptide, ser17 substitution for continuous cell lines was compared with that of native, human IFN- ⁇ .
  • T24 cells derived from a transitional cell carcinoma were treated with 200 units/ml of the proteins. Cell growth was inhibited significantly. (p>0.2) by both proteins. This procedure and results were described in Mark et al., Proc. Natl. Acad. Sci. USA 81: 5662-5666 (1984 ).
  • IFN- ⁇ polypeptide ser17 substitution
  • NK natural killer cell
  • the IFN- ⁇ polypeptide was tested with two cell types: (1) Ficoll-hypaque separated peripheral human mononuclear cells (PMC); or (2) NK-enriched lymphocyte preparations depleted of monocytes by plastic adherence and of OKT3-positive T cells by treatment with OKT3 antibody plus complement.
  • PMC Ficoll-hypaque separated peripheral human mononuclear cells
  • NK-enriched lymphocyte preparations depleted of monocytes by plastic adherence and of OKT3-positive T cells by treatment with OKT3 antibody plus complement.
  • the cells were incubated overnight in growth medium containing various concentrations of IFN- ⁇ polypeptide, ser17 substitution.
  • 51 CR-labeled target cells were incubated with the effector cells for 2-4 hours.
  • the effector cell to target cell ratio was 50:1.
  • NK cell cytoxicity was determined by measuring the amount of label released into the medium. This procedure and results were described in Mark et al., Proc. Natl. Acad. Sci. USA 81: 5662-5666 (1984 ).
  • This experiment relates to fermentation of a cell capable of producing IFN- ⁇ polypeptide under conditions of high potassium and sodium cation concentrations, and glucose as the effective non-limiting energy source. Further, the cells were cultured at 37°C and pH 6.8 with KOH as a titrant.
  • the cells were maintained at pH 6.8 throughout the fermentation using potassium hydroxide as a titrant. Further, the cells were cultured at 37°C at 40% dissolved oxygen.
  • IFN- ⁇ polypeptide concentration was determined by SDS-PAGE analysis with a IFN- ⁇ polypeptide standard. Total protein content was assayed using a standard Lowry protocol.
  • E.coli, strain MM294 cells transformed with pSY2501, described in Example 1 were cultured in the basal medium, below, with varying concentrations of potassium cations with a fixed concentration of sodium cations.
  • the cells were cultured in one of three media described below: ⁇ 40 mM Potassium Cation Medium 4.4 mM potassium citrate 26.8 mM KH 2 PO 4 66.8 mM (NH 4 ) 2 SO 4 33.2 mM NH 4 H 2 PO 4 10 mM MgSO 4 2 g/L glucose 20 g/L glycerol 140 mg/L tryptophan 24 mg/L thiamine 4.7 mL/L BTM (trace elements) ⁇ 75 mM Potassium Cation Medium 4.4 mM potassium citrate 35 mM KH 2 PO 4 72 mM (NH 4 ) 2 SO 4 5 mM MgSO 4 2 g/L glucose 20 g/L glycerol 30 mM KCl 70 mg/L tryptophan 24 mg/L thiamine 50 mg/L ampicillin 4.7 mL/L BTM (trace elements) 5 mM MgSO 4 and 15 mM KH 2 PO 4 were added at 40
  • the fermentation medium was maintained at a pH of 5.7 with 7.4 N NH 4 OH. Fifty percent (v/v) glycerol was fed at a 3.5:1 ratio with the ammonium hydroxide. The initial glycerol volume in the feed reservoir should be 150 mL/L of fermentor working volume. The temperature was maintained at 37°C. The cells were harvested seven hours after reaching an optical density of 16 OD 680 units.
  • Each culture contained one of the following approximately concentrations of potassium cations: 40 mM, 75 mM, and 120 mM.
  • the resulting-growth rates and IEN- ⁇ polypeptide production rates of each culture are shown in Figure 1 .
  • the 75 mM culture reached an optical density (OD 680 ) of approximately 85 units compared to approximately 35 units, more than a two fold difference, than the 120 mM culture.
  • the 75 mM culture grew to a higher cell density than the 40 mM culture, the 40 mM culture produced almost 2000 ⁇ g/mL of IFN- ⁇ polypeptide in contrast to the 75 mM culture which only produced somewhat less than 1200 ⁇ g/mL.
  • the production of IFN- ⁇ polypeptide increased approximately 60% when 40 mM K + was used instead of 75 mM K + .
  • the 120 mM culture produced almost no IFN- ⁇ polypeptide.
  • IFN- ⁇ polypeptide The production levels of IFN- ⁇ polypeptide was measured by SDS-PAGE analysis stained with Coomassie.
  • E.coli, strain MM294 cells transformed with pSY2501, described in Example 1 were cultured in the basal medium, below, with varying amounts of potassium and sodium cations added.
  • the cells were cultured in a fermentor until exponential growth phase in defined medium containing tryptophan. The cells were then inoculated at the desired cell density in the above basal media with the desired concentration of potassium and sodium cations. This media were added to sterilized shake flasks.
  • Each culture contained one of the following concentrations of potassium and sodium salts, 40 mM K + /0 mM Na + , 30 mM K + /10 mM Na + , 20 mM K + /20 mM Na + , 10 mM K + /30 mM Na + , 0 mM K + /40 mM Na + .
  • the resulting IFN- ⁇ polypeptide production rate of each culture is shown in Figure 2 .
  • the culture with no K + cations and 40 mM Na + produced approximately 50 ⁇ g of IFN- ⁇ polypeptide per mg of total cell protein.
  • the culture with 40 mM K + /0 mM Na + produced approximately 90 ⁇ g of IFN- ⁇ polypeptide per mg of total cell protein. This is approximately a 80% improvement in yield.
  • the IFN- ⁇ polypeptide concentration was measured by ELISA.
  • the total protein concentration was assayed using a BCA assay, Pierce Chemical. Cell density was measured using Klett units.
  • E.coli, strain MM294-1 cells transformed with pSY2501, described in Example 1, were cultured in the basal medium, below, titrated to varying pH.
  • E.coli, strain MM294 cells transformed with pSY2501, described in Example 1 were cultured in the medium, below, with either glycerol, fructose, or glucose as the effective, non-limiting energy source.
  • the IFN- ⁇ polypeptide concentration was measured by SDS-PAGE analysis with a IFN- ⁇ polypeptide standard.
  • E.coli, strain MM294 cells transformed with pSY2501, described in Example 1, were cultured in the medium, below, at varying temperatures:
  • the fermentation medium was maintained at a pH of 5.7 with 7.4 N NH 4 OH. Fifty percent (v/v) glycerol is feed at a 3.5:1 ratio with the ammonium hydroxide. The temperature was maintained at 34 or 37 or 40°C.
  • the growth rates of the different cultures did not vary greatly. However, as the temperature increased, the yield of IFN- ⁇ polypeptide compared to total cell protein also increased. At 34°C, 8.5% of the protein produced was IFN- ⁇ polypeptide. At 37°C and 40°C, 10.5% and 13.5%, respectively, of the total protein produced was IFN- ⁇ polypeptide. In the control experiment, described in Example 2, only 5.1 % of the total protein was IFN- ⁇ polypeptide.
  • the IFN- ⁇ polypeptide concentration was measured by SDS-PAGE analysis with a IFN- ⁇ polypeptide standard. The total protein concentration was assayed by BCA.
  • the following fermentation procedure incorporated low potassium and sodium cation concentrations, low pH, high temperature, and glycerol as the effective non-limiting energy source.
  • the average IFN- ⁇ polypeptide production from this fermentation procedure is 5 to 6 fold better than the production of the procedure described in Example 2.
  • BTM is a trace element mixture.
  • the composition of BTM is as follows:
  • This solution was added to a sterilized fermentor containing approximately 7.0 L of DI water. Next, the solution in the fermentor was brought to a final volume of 9.0 L with DI water. Ten mL of PPG antifoam was added and the fermentor was inoculated with 10 - 20 mg (dry weight) of cells.
  • the fermentation medium was maintained at a pH of 5.7 with 7.4 N NH 4 OH.
  • Fifty percent (v/v) glycerol was fed at a 3.5:1 ratio with the ammonium hydroxide.
  • Leucine and isoleucine were also fed to the host cells with the glycerol and the base. These amino acids were fed by adding to 26.4 g of isoleucine and 19.7 g of leucine to every 700 mLs of 7.4 N NH 4 OH. This mixture of base and amino acids was used to maintain the pH of the culture medium.
  • the initial glycerol volume in the feed reservoir should be 1500 mL.
  • the temperature was maintained at 39.5°C.
  • the cells were harvested seven hours after reaching an optical density of 16 OD 680 units.
  • a typical fermentation run following these procedures produced an average of -2.0 - 2.5 g/L IFN- ⁇ polypeptide compared to the control fermentation, described in Example 2, which produced an average of 0.35 g/L. These fermentation conditions produce over 5-6 fold more IFN- ⁇ polypeptide than the control fermentation conditions. Further, an average of ⁇ 11.5% of the total cell protein, utilizing these procedures, is IFN- ⁇ polypeptide compared to an average of ⁇ 5.1% in the control fermentation. Thus, the IFN- ⁇ polypeptide produced by this procedure has approximately over 2 fold increase of purity.

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  • Peptides Or Proteins (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (14)

  1. Verfahren zur Produktion von Interferon-β in Escherichia coli, umfassend:
    (a) Bereitstellen einer Escherichia-coli-Wirtszelle, transformiert mit einem Vektor, der eine Sequenz, die für ein Interferon-β-Polypeptid codiert, umfasst, und
    (b) Kultivieren der Zelle unter Bedingungen, die wirksam sind zum Induzieren der Produktion von Interferon-β-Polypeptid, in einem Medium, das nicht mehr als 75 mM an Kaliumionen und nicht mehr als 100 µM an Natriumkationen umfasst, wobei der pH des Mediums zwischen 5,4 und 6,0 gehalten wird.
  2. Verfahren nach Anspruch 1, wobei die Kaliumkation-Konzentration nicht mehr als 40 mM beträgt.
  3. Verfahren nach Anspruch 1, wobei die Kaliumkation-Konzentration nicht weniger als 10 mM beträgt.
  4. Verfahren nach Anspruch 1, wobei die Kaliumkation-Konzentration nicht mehr als 40 mM und nicht weniger als 10 mM beträgt.
  5. Verfahren nach Anspruch 1, wobei die Natriumkation-Konzentration nicht mehr als 50 µM beträgt.
  6. Verfahren nach Anspruch 1, wobei das Medium Glycerin als eine wirksame Energiequelle umfasst und bei einem pH zwischen 5,4 und 5,7 gehalten wird und die Kulturbedingungen Kultivieren der Zelle bei einer Temperatur von 39,5°C umfassen.
  7. Verfahren nach Anspruch 1, wobei das Medium Glycerin umfasst.
  8. Verfahren nach Anspruch 7, wobei die Glycerinkonzentration zwischen 2 g/L und 100 g/L liegt.
  9. Verfahren nach Anspruch 1, wobei die Kulturbedingungen Kultivieren der Zelle zwischen 34°C und 42°C umfassen.
  10. Verfahren nach Anspruch 1 oder 7, wobei das Medium des Weiteren eine Menge an Glucose umfasst.
  11. Verfahren nach Anspruch 1, wobei die Aminosäuresequenz des Interferon-β-Polypeptids SEQ ID NO:1 ist, worin Aminosäure 17 Serin ist.
  12. Verfahren nach Anspruch 12, wobei die Wirtszelle Escherichia coli, Stamm MM 294-1 ist.
  13. Verfahren nach Anspruch 12, wobei der Vektor pSY2501 (ATCC-Eingangsnummer 39517) ist.
  14. Zusammensetzung zum Produzieren von IFN-β-Polypeptid, umfassend:
    (a) eine Escherichia-coli-Zelle, die zur IFN-β-Produktion befähigt ist, und
    (b) ein Kulturmedium, umfassend:
    (i) nicht mehr als 75 mM K+-Kationen,
    (ii) nicht mehr als 100 µM Na+-Kationen und
    (iii) zwischen 2 und 100 g/L Glycerin;
    wobei der pH des Kulturmediums zwischen 5,4 und 5,7 beträgt.
EP96919131A 1995-06-06 1996-06-05 Bakterielle Produktion von Interferon-beta Polypeptiden Expired - Lifetime EP0778893B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/477,310 US5814485A (en) 1995-06-06 1995-06-06 Production of interferon-β (IFN-β) in E. coli
US477310 1995-06-06
PCT/US1996/009155 WO1996039523A2 (en) 1995-06-06 1996-06-05 Bacterial production of hydrophobic polypeptides

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EP0778893B1 true EP0778893B1 (de) 2009-11-18

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EP (1) EP0778893B1 (de)
JP (3) JP4131554B2 (de)
AT (1) ATE449175T1 (de)
AU (1) AU6154996A (de)
BR (1) BR9606491A (de)
CA (1) CA2195799C (de)
DE (1) DE69638077D1 (de)
FI (1) FI970445A (de)
IL (1) IL120009A0 (de)
IN (1) IN190514B (de)
MX (1) MX9700818A (de)
MY (1) MY118492A (de)
NO (1) NO324529B1 (de)
NZ (1) NZ310710A (de)
TW (1) TW494138B (de)
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WO2004022593A2 (en) * 2002-09-09 2004-03-18 Nautilus Biotech Rational evolution of cytokines for higher stability, the cytokines and encoding nucleic acid molecules
BRPI0412477A (pt) 2003-07-11 2006-09-19 Schering Ag aperfeiçoados polipeptìdeos de interferon-beta-1b recombinantes humanos
ES2374530T3 (es) * 2003-12-11 2012-02-17 Ares Trading S.A. Formulaciones líquidas de interferón estabilizado.
US8906676B2 (en) 2004-02-02 2014-12-09 Ambrx, Inc. Modified human four helical bundle polypeptides and their uses
US20080076729A1 (en) * 2005-05-19 2008-03-27 Schering Aktiengesellachaft Interferon-beta gene therapy using an improved, regulated expression system
PE20061416A1 (es) * 2005-05-19 2007-01-26 Schering Ag Sistema de expresion genetica que comprende un interferon-beta
US20070179113A1 (en) * 2005-05-19 2007-08-02 Schering Aktiengesellachaft GM-CSF gene therapy for Crohn's disease using an improved regulated expression system
US20060281703A1 (en) * 2005-05-19 2006-12-14 Schering Aktiengesellschaft Treatment of disease using an improved regulated expression system
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WO2008130382A2 (en) 2006-10-31 2008-10-30 East Carolina University Fusion proteins comprising an anti -inflammatory cytokine and an antigen for treatment of immune disorders
WO2008125222A2 (en) * 2007-04-11 2008-10-23 Bayer Schering Pharma Aktiengesellschaft New modulation molecules for an improved regulated expression system
AU2008247815B2 (en) 2007-05-02 2012-09-06 Ambrx, Inc. Modified interferon beta polypeptides and their uses
EP2207890A4 (de) * 2007-10-05 2010-12-15 Barofold Inc Hochdruckbehandlung aggregierter interferone
JP5563475B2 (ja) * 2007-12-20 2014-07-30 メルク セローノ ソシエテ アノニム Ｐｅｇインターフェロン−ベータ製剤
CN103694337B (zh) 2008-02-08 2016-03-02 Ambrx公司 经修饰瘦素多肽和其用途
KR20090124204A (ko) * 2008-05-29 2009-12-03 (주)바이오큐어팜 아미노 말단의 메티오닌이 제거된 재조합 사람 변이인터페론-베타 단백질을 생산하는 재조합 대장균 및 이의제조방법
CA2757287C (en) * 2009-03-31 2019-09-10 East Carolina University Cytokines and neuroantigens for treatment of immune disorders
CA2788607C (en) * 2010-02-01 2018-03-20 Digna Biotech,S.L. Process for the production of interferon alpha 5
ES2639398T3 (es) * 2010-03-04 2017-10-26 Pfenex Inc. Método para producir proteína de interferón recombinante soluble sin desnaturalización
RU2473696C1 (ru) * 2011-07-14 2013-01-27 Закрытое акционерное общество "ГЕНЕРИУМ" ПРОМЫШЛЕННЫЙ СПОСОБ ПОЛУЧЕНИЯ И ОЧИСТКИ РЕКОМБИНАНТНОГО ИНТЕРФЕРОНА β-1b ЧЕЛОВЕКА ИЗ ТЕЛЕЦ ВКЛЮЧЕНИЯ
JP6363326B2 (ja) * 2013-03-11 2018-07-25 株式会社コーセー 酵母・細菌共通培養方法およびこれに用いる酵母・細菌共通培養培地
JP7151049B2 (ja) * 2018-03-30 2022-10-12 三井化学株式会社 微生物を増殖させる方法

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NO970514D0 (no) 1997-02-05
JP4317890B2 (ja) 2009-08-19
US5814485A (en) 1998-09-29
EP0778893A2 (de) 1997-06-18
CA2195799A1 (en) 1996-12-12
NZ310710A (en) 1999-01-28
WO1996039523A2 (en) 1996-12-12
JPH11501820A (ja) 1999-02-16
MX9700818A (es) 1997-05-31
TW494138B (en) 2002-07-11
DE69638077D1 (de) 2009-12-31
ATE449175T1 (de) 2009-12-15
IN190514B (de) 2003-08-02
FI970445A (fi) 1997-03-26
AU6154996A (en) 1996-12-24
NO324529B1 (no) 2007-11-12
WO1996039523A3 (en) 1997-01-30
CA2195799C (en) 2010-02-09
MY118492A (en) 2004-11-30
FI970445A0 (fi) 1997-02-03
JP4131554B2 (ja) 2008-08-13
BR9606491A (pt) 1997-09-02
NO970514L (no) 1997-03-17
JP2008086331A (ja) 2008-04-17
IL120009A0 (en) 1997-04-15
JP2008283988A (ja) 2008-11-27

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